A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515091



Internal ID20888448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51397392..51397763hg38UCSC Ensembl
chr16:51431303..51431674hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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